{"count":220828,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=730","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=728","results":[{"created":"2022-10-06T11:44:59.901515+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.371","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mpl has been classified as Green List (High Evidence).","entity_name":"MPL","entity_type":"gene"},{"created":"2022-10-06T11:44:56.251452+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.371","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MPL were changed from Thrombocytopaenia, congenital amegakaryocytic, MIM# 604498 to Thrombocytopenia, congenital amegakaryocytic, MIM# 604498","entity_name":"MPL","entity_type":"gene"},{"created":"2022-10-06T11:44:46.500413+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.370","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MPL were changed from Amegakaryocytic thrombocytopaenia, congenital to Thrombocytopaenia, congenital amegakaryocytic, MIM# 604498","entity_name":"MPL","entity_type":"gene"},{"created":"2022-10-06T11:44:32.447496+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.369","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MPL were set to ","entity_name":"MPL","entity_type":"gene"},{"created":"2022-10-06T11:44:19.507452+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.368","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MPL: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Thrombocytopenia, congenital amegakaryocytic, MIM# 604498; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MPL","entity_type":"gene"},{"created":"2022-10-06T11:43:37.315747+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.368","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MPI as ready","entity_name":"MPI","entity_type":"gene"},{"created":"2022-10-06T11:43:37.307045+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.368","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mpi has been classified as Green List (High Evidence).","entity_name":"MPI","entity_type":"gene"},{"created":"2022-10-06T11:43:33.615570+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.368","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MPI were changed from Congenital disorder of glycosylation 1b to Congenital disorder of glycosylation, type Ib, MIM# 602579","entity_name":"MPI","entity_type":"gene"},{"created":"2022-10-06T11:43:19.914259+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.367","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MPI were set to ","entity_name":"MPI","entity_type":"gene"},{"created":"2022-10-06T11:43:05.667448+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.366","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MPI: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Congenital disorder of glycosylation, type Ib, MIM# 602579; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MPI","entity_type":"gene"},{"created":"2022-10-06T11:42:24.780690+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.366","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MPDU1 as ready","entity_name":"MPDU1","entity_type":"gene"},{"created":"2022-10-06T11:42:24.768405+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.366","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mpdu1 has been classified as Red List (Low Evidence).","entity_name":"MPDU1","entity_type":"gene"},{"created":"2022-10-06T11:42:14.040808+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.366","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MPDU1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Congenital disorder of glycosylation, type If, MIM# 609180; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MPDU1","entity_type":"gene"},{"created":"2022-10-06T11:41:54.278852+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.366","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MPDU1 as Red List (low evidence)","entity_name":"MPDU1","entity_type":"gene"},{"created":"2022-10-06T11:41:54.267896+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.366","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mpdu1 has been classified as Red List (Low Evidence).","entity_name":"MPDU1","entity_type":"gene"},{"created":"2022-10-06T11:41:18.693931+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.365","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MOCS2 as ready","entity_name":"MOCS2","entity_type":"gene"},{"created":"2022-10-06T11:41:18.685667+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.365","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mocs2 has been classified as Red List (Low Evidence).","entity_name":"MOCS2","entity_type":"gene"},{"created":"2022-10-06T11:41:13.885419+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.365","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MOCS2 were changed from Molybdenum cofactor deficiency to Molybdenum cofactor deficiency B, MIM#252160","entity_name":"MOCS2","entity_type":"gene"},{"created":"2022-10-06T11:40:56.738013+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.364","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MOCS2 as Red List (low evidence)","entity_name":"MOCS2","entity_type":"gene"},{"created":"2022-10-06T11:40:56.728788+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.364","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mocs2 has been classified as Red List (Low Evidence).","entity_name":"MOCS2","entity_type":"gene"},{"created":"2022-10-06T11:40:43.782673+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.363","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MOCS2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Molybdenum cofactor deficiency B MIM#252160; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MOCS2","entity_type":"gene"},{"created":"2022-10-06T11:39:48.529372+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.346","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: MOCS1.","entity_name":"MOCS1","entity_type":"gene"},{"created":"2022-10-06T11:39:21.183469+11:00","panel_name":"Miscellaneous Metabolic Disorders","panel_id":3468,"panel_version":"1.23","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: MOCS1.","entity_name":"MOCS1","entity_type":"gene"},{"created":"2022-10-06T11:39:01.733611+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4959","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: MOCS1.","entity_name":"MOCS1","entity_type":"gene"},{"created":"2022-10-06T11:38:44.549051+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1675","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: MOCS1.","entity_name":"MOCS1","entity_type":"gene"},{"created":"2022-10-06T11:38:30.548894+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.363","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MOCS1 as ready","entity_name":"MOCS1","entity_type":"gene"},{"created":"2022-10-06T11:38:30.538285+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.363","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mocs1 has been classified as Green List (High Evidence).","entity_name":"MOCS1","entity_type":"gene"},{"created":"2022-10-06T11:38:24.777766+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.363","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MOCS1 were set to ","entity_name":"MOCS1","entity_type":"gene"},{"created":"2022-10-06T11:38:04.340224+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.362","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MOCS1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Molybdenum cofactor deficiency A, MIM# 252150; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MOCS1","entity_type":"gene"},{"created":"2022-10-06T11:37:07.427541+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.362","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: MOCS1.","entity_name":"MOCS1","entity_type":"gene"},{"created":"2022-10-06T11:36:39.377649+11:00","panel_name":"Hyperammonaemia","panel_id":3470,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: MLYCD.","entity_name":"MLYCD","entity_type":"gene"},{"created":"2022-10-06T11:36:23.146094+11:00","panel_name":"Cardiomyopathy_Paediatric","panel_id":3270,"panel_version":"0.134","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: MLYCD.","entity_name":"MLYCD","entity_type":"gene"},{"created":"2022-10-06T11:36:04.198032+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4959","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: MLYCD.","entity_name":"MLYCD","entity_type":"gene"},{"created":"2022-10-06T11:35:28.875782+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.346","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: MLYCD.","entity_name":"MLYCD","entity_type":"gene"},{"created":"2022-10-06T11:35:10.683821+11:00","panel_name":"Fatty Acid Oxidation Defects","panel_id":103,"panel_version":"1.8","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: MLYCD.","entity_name":"MLYCD","entity_type":"gene"},{"created":"2022-10-06T11:34:52.985697+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.362","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: MLYCD.","entity_name":"MLYCD","entity_type":"gene"},{"created":"2022-10-06T11:34:12.848549+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.362","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MLYCD as ready","entity_name":"MLYCD","entity_type":"gene"},{"created":"2022-10-06T11:34:12.838677+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.362","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mlycd has been classified as Green List (High Evidence).","entity_name":"MLYCD","entity_type":"gene"},{"created":"2022-10-06T11:34:09.248931+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.362","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MLYCD were changed from Malonyl-CoA decarboxylase deficiency to Malonyl-CoA decarboxylase deficiency, MIM# 248360","entity_name":"MLYCD","entity_type":"gene"},{"created":"2022-10-06T11:33:53.704547+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.361","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MLYCD: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Malonyl-CoA decarboxylase deficiency, MIM# 248360; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MLYCD","entity_type":"gene"},{"created":"2022-10-06T11:33:05.993804+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.361","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ZAP70 as ready","entity_name":"ZAP70","entity_type":"gene"},{"created":"2022-10-06T11:33:05.983802+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.361","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: zap70 has been classified as Green List (High Evidence).","entity_name":"ZAP70","entity_type":"gene"},{"created":"2022-10-06T11:33:02.248672+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.361","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ZAP70 were changed from ZAP70-related severe combined immunodeficiency to Immunodeficiency MIM#176947","entity_name":"ZAP70","entity_type":"gene"},{"created":"2022-10-06T11:32:50.727823+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.360","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ZAP70 were set to ","entity_name":"ZAP70","entity_type":"gene"},{"created":"2022-10-06T11:32:40.283300+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.359","user_name":"Zornitza Stark","item_type":"entity","text":"Tag treatable tag was added to gene: ZAP70.","entity_name":"ZAP70","entity_type":"gene"},{"created":"2022-10-06T11:32:14.928400+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.359","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ZEB2 as ready","entity_name":"ZEB2","entity_type":"gene"},{"created":"2022-10-06T11:32:14.916904+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.359","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: zeb2 has been classified as Red List (Low Evidence).","entity_name":"ZEB2","entity_type":"gene"},{"created":"2022-10-06T11:32:09.931325+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.359","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ZEB2 were changed from Mowat-Wilson syndrome to Mowat-Wilson syndrome MIM# 235730","entity_name":"ZEB2","entity_type":"gene"},{"created":"2022-10-06T11:31:58.815865+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.358","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ZEB2 were set to ","entity_name":"ZEB2","entity_type":"gene"},{"created":"2022-10-06T11:31:47.997874+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.357","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ZEB2 as Red List (low evidence)","entity_name":"ZEB2","entity_type":"gene"},{"created":"2022-10-06T11:31:47.988554+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.357","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: zeb2 has been classified as Red List (Low Evidence).","entity_name":"ZEB2","entity_type":"gene"},{"created":"2022-10-06T11:31:24.274552+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.356","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ZIC2 as ready","entity_name":"ZIC2","entity_type":"gene"},{"created":"2022-10-06T11:31:24.265025+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.356","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: zic2 has been classified as Red List (Low Evidence).","entity_name":"ZIC2","entity_type":"gene"},{"created":"2022-10-06T11:31:19.922818+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.356","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ZIC2 were changed from Holoprosencephaly-5 to Holoprosencephaly MIM#603073","entity_name":"ZIC2","entity_type":"gene"},{"created":"2022-10-06T11:31:04.916010+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.355","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ZIC2 were set to ","entity_name":"ZIC2","entity_type":"gene"},{"created":"2022-10-06T11:30:54.388561+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.354","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ZIC2 as Red List (low evidence)","entity_name":"ZIC2","entity_type":"gene"},{"created":"2022-10-06T11:30:54.381287+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.354","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: zic2 has been classified as Red List (Low Evidence).","entity_name":"ZIC2","entity_type":"gene"},{"created":"2022-10-06T11:30:28.015262+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.353","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ZIC3 as ready","entity_name":"ZIC3","entity_type":"gene"},{"created":"2022-10-06T11:30:28.006315+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.353","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: zic3 has been classified as Red List (Low Evidence).","entity_name":"ZIC3","entity_type":"gene"},{"created":"2022-10-06T11:30:24.527626+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.353","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ZIC3 were changed from Heterotaxy to X linked heterotaxy and congenital heart defects MIM:306955","entity_name":"ZIC3","entity_type":"gene"},{"created":"2022-10-06T11:30:14.304706+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.352","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ZIC3 were set to ","entity_name":"ZIC3","entity_type":"gene"},{"created":"2022-10-06T11:29:59.657694+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.351","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ZIC3 as Red List (low evidence)","entity_name":"ZIC3","entity_type":"gene"},{"created":"2022-10-06T11:29:59.647771+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.351","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: zic3 has been classified as Red List (Low Evidence).","entity_name":"ZIC3","entity_type":"gene"},{"created":"2022-10-06T11:29:11.095890+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.350","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ZMPSTE24 as ready","entity_name":"ZMPSTE24","entity_type":"gene"},{"created":"2022-10-06T11:29:11.087396+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.350","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: zmpste24 has been classified as Red List (Low Evidence).","entity_name":"ZMPSTE24","entity_type":"gene"},{"created":"2022-10-06T11:29:07.479046+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.350","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ZMPSTE24 were changed from Restrictive dermopathy to Restrictive dermopathy 1, MIM# MIM:275210","entity_name":"ZMPSTE24","entity_type":"gene"},{"created":"2022-10-06T11:28:56.296655+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.349","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ZMPSTE24 were set to ","entity_name":"ZMPSTE24","entity_type":"gene"},{"created":"2022-10-06T11:28:42.856571+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.348","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ZMPSTE24 as Red List (low evidence)","entity_name":"ZMPSTE24","entity_type":"gene"},{"created":"2022-10-06T11:28:42.848702+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.348","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: zmpste24 has been classified as Red List (Low Evidence).","entity_name":"ZMPSTE24","entity_type":"gene"},{"created":"2022-10-06T11:28:21.222842+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.347","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ZMPSTE24: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Restrictive dermopathy 1, MIM# MIM:275210; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"ZMPSTE24","entity_type":"gene"},{"created":"2022-10-06T11:27:34.885480+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.347","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ZNF469 as ready","entity_name":"ZNF469","entity_type":"gene"},{"created":"2022-10-06T11:27:34.876115+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.347","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: znf469 has been classified as Red List (Low Evidence).","entity_name":"ZNF469","entity_type":"gene"},{"created":"2022-10-06T11:27:30.647424+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.347","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ZNF469 were changed from Brittle cornea syndrome to Brittle cornea syndrome MIM#229200","entity_name":"ZNF469","entity_type":"gene"},{"created":"2022-10-06T11:27:17.568549+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.346","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ZNF469 were set to ","entity_name":"ZNF469","entity_type":"gene"},{"created":"2022-10-06T11:27:07.611804+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.345","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ZNF469 as Red List (low evidence)","entity_name":"ZNF469","entity_type":"gene"},{"created":"2022-10-06T11:27:07.602149+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.345","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: znf469 has been classified as Red List (Low Evidence).","entity_name":"ZNF469","entity_type":"gene"},{"created":"2022-10-06T11:26:22.551135+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.344","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MLC1 as ready","entity_name":"MLC1","entity_type":"gene"},{"created":"2022-10-06T11:26:22.541378+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.344","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mlc1 has been classified as Red List (Low Evidence).","entity_name":"MLC1","entity_type":"gene"},{"created":"2022-10-06T11:26:18.304707+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.344","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MLC1 were changed from Megalencephalic leukoencephalopathy to Megalencephalic leukoencephalopathy with subcortical cysts OMIM#604004","entity_name":"MLC1","entity_type":"gene"},{"created":"2022-10-06T11:26:04.977295+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.343","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MLC1 as Red List (low evidence)","entity_name":"MLC1","entity_type":"gene"},{"created":"2022-10-06T11:26:04.969424+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.343","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mlc1 has been classified as Red List (Low Evidence).","entity_name":"MLC1","entity_type":"gene"},{"created":"2022-10-06T11:25:53.349661+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.342","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MLC1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Megalencephalic leukoencephalopathy with subcortical cysts OMIM#604004; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MLC1","entity_type":"gene"},{"created":"2022-10-06T11:25:16.727093+11:00","panel_name":"Skeletal Dysplasia_Fetal","panel_id":28,"panel_version":"0.136","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NANS as ready","entity_name":"NANS","entity_type":"gene"},{"created":"2022-10-06T11:25:16.717880+11:00","panel_name":"Skeletal Dysplasia_Fetal","panel_id":28,"panel_version":"0.136","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nans has been classified as Green List (High Evidence).","entity_name":"NANS","entity_type":"gene"},{"created":"2022-10-06T11:25:11.678739+11:00","panel_name":"Skeletal Dysplasia_Fetal","panel_id":28,"panel_version":"0.136","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NANS as Green List (high evidence)","entity_name":"NANS","entity_type":"gene"},{"created":"2022-10-06T11:25:11.667537+11:00","panel_name":"Skeletal Dysplasia_Fetal","panel_id":28,"panel_version":"0.136","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nans has been classified as Green List (High Evidence).","entity_name":"NANS","entity_type":"gene"},{"created":"2022-10-06T11:24:26.043012+11:00","panel_name":"Skeletal Dysplasia_Fetal","panel_id":28,"panel_version":"0.135","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NBAS as ready","entity_name":"NBAS","entity_type":"gene"},{"created":"2022-10-06T11:24:26.032140+11:00","panel_name":"Skeletal Dysplasia_Fetal","panel_id":28,"panel_version":"0.135","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nbas has been classified as Green List (High Evidence).","entity_name":"NBAS","entity_type":"gene"},{"created":"2022-10-06T11:24:21.992405+11:00","panel_name":"Skeletal Dysplasia_Fetal","panel_id":28,"panel_version":"0.135","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NBAS as Green List (high evidence)","entity_name":"NBAS","entity_type":"gene"},{"created":"2022-10-06T11:24:21.982808+11:00","panel_name":"Skeletal Dysplasia_Fetal","panel_id":28,"panel_version":"0.135","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nbas has been classified as Green List (High Evidence).","entity_name":"NBAS","entity_type":"gene"},{"created":"2022-10-06T11:23:35.163038+11:00","panel_name":"Skeletal Dysplasia_Fetal","panel_id":28,"panel_version":"0.134","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NPR2 as ready","entity_name":"NPR2","entity_type":"gene"},{"created":"2022-10-06T11:23:35.155062+11:00","panel_name":"Skeletal Dysplasia_Fetal","panel_id":28,"panel_version":"0.134","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: npr2 has been classified as Amber List (Moderate Evidence).","entity_name":"NPR2","entity_type":"gene"},{"created":"2022-10-06T11:23:30.824740+11:00","panel_name":"Skeletal Dysplasia_Fetal","panel_id":28,"panel_version":"0.134","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NPR2 as Amber List (moderate evidence)","entity_name":"NPR2","entity_type":"gene"},{"created":"2022-10-06T11:23:30.816557+11:00","panel_name":"Skeletal Dysplasia_Fetal","panel_id":28,"panel_version":"0.134","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: npr2 has been classified as Amber List (Moderate Evidence).","entity_name":"NPR2","entity_type":"gene"},{"created":"2022-10-06T11:22:58.954079+11:00","panel_name":"Skeletal Dysplasia_Fetal","panel_id":28,"panel_version":"0.133","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NPR2: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Acromesomelic dysplasia 1, Maroteaux type - MIM#602875; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NPR2","entity_type":"gene"},{"created":"2022-10-06T11:21:44.225467+11:00","panel_name":"Skeletal Dysplasia_Fetal","panel_id":28,"panel_version":"0.133","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NPR2 as Green List (high evidence)","entity_name":"NPR2","entity_type":"gene"},{"created":"2022-10-06T11:21:44.217545+11:00","panel_name":"Skeletal Dysplasia_Fetal","panel_id":28,"panel_version":"0.133","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: npr2 has been classified as Green List (High Evidence).","entity_name":"NPR2","entity_type":"gene"},{"created":"2022-10-06T11:20:57.647223+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.342","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MKS1 as ready","entity_name":"MKS1","entity_type":"gene"},{"created":"2022-10-06T11:20:57.638886+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.342","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mks1 has been classified as Red List (Low Evidence).","entity_name":"MKS1","entity_type":"gene"},{"created":"2022-10-06T11:20:53.717535+11:00","panel_name":"gNBS","panel_id":3931,"panel_version":"0.342","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MKS1 were changed from Meckel syndrome to Joubert syndrome 28, MIM# 617121 MONDO:0014928; Meckel syndrome 1, MIM# 249000 MONDO:0009571; Bardet-Biedl syndrome 13, MIM# 615990 MONDO:0014441","entity_name":"MKS1","entity_type":"gene"}]}